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GTR Home > Conditions/Phenotypes > ALG9 congenital disorder of glycosylation

Summary

Congenital disorders of glycosylation (CDGs) that represent defects of dolichol-linked oligosaccharide assembly are classified as CDG type I. For a general description and a discussion of the classification of CDGs, see CDG1A (212065). [from OMIM]

Available tests

40 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Genes See tests for all associated and related genes

  • Also known as: CDG1L, DIBD1, GIKANIS, LOH11CR1J, ALG9
    Summary: ALG9 alpha-1,2-mannosyltransferase

Clinical features

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